Canonical Allele Identifier: CA348704056

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145154048C>T (hg19) ; chr2:g.144396481C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396481C>T , CM000664.2:g.144396481C>T	GRCh38
NC_000002.11:g.145154048C>T , CM000664.1:g.145154048C>T	GRCh37
NC_000002.10:g.144870518C>T	NCBI36
NG_016431.1:g.128911G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2847G>A	ENSP00000508434.1:n.*2847G>A
ENST00000440875.6:c.2221G>A	ENSP00000475553.3:p.Ala741Thr
ENST00000627532.3:c.2998G>A MANE Select	ENSP00000487174.1:p.Ala1000Thr
ENST00000636026.2:c.2998G>A	ENSP00000490776.1:p.Ala1000Thr
ENST00000636179.1:n.2967G>A
ENST00000636413.1:c.2662G>A	ENSP00000490508.1:p.Ala888Thr
ENST00000636471.1:c.3073G>A	ENSP00000490317.1:p.Ala1025Thr
ENST00000636732.2:c.*2715G>A	ENSP00000490175.1:n.*2715G>A
ENST00000636820.1:n.3098G>A
ENST00000637045.1:c.2662G>A	ENSP00000490141.1:p.Ala888Thr
ENST00000637304.1:c.2662G>A	ENSP00000490872.1:p.Ala888Thr
ENST00000638007.1:c.2662G>A	ENSP00000490723.1:p.Ala888Thr
ENST00000638087.1:c.2662G>A	ENSP00000490673.1:p.Ala888Thr
ENST00000638128.1:c.2221G>A	ENSP00000490934.1:p.Ala741Thr
ENST00000639389.1:c.82G>A	ENSP00000492572.1:p.Ala28Thr
ENST00000647488.1:c.130G>A	ENSP00000494820.1:p.Ala44Thr
ENST00000675069.1:c.529G>A	ENSP00000502467.1:p.Ala177Thr
ENST00000303660.8:c.2995G>A	ENSP00000302501.4:p.Ala999Thr
ENST00000409487.7:c.2998G>A	ENSP00000386854.2:p.Ala1000Thr
ENST00000419938.5:c.655+4718G>A	ENSP00000394777.2:n.655+4718G>A
ENST00000539609.7:c.2926G>A	ENSP00000443792.2:p.Ala976Thr
ENST00000558170.6:c.2998G>A	ENSP00000454157.1:p.Ala1000Thr
ENST00000627532.2:c.2998G>A	ENSP00000487174.1:p.Ala1000Thr
NM_001171653.1:c.2926G>A	NP_001165124.1:p.Ala976Thr
NM_014795.3:c.2998G>A	NP_055610.1:p.Ala1000Thr
XM_006712881.2:c.2998G>A	XP_006712944.1:p.Ala1000Thr
XM_006712882.2:c.2998G>A	XP_006712945.1:p.Ala1000Thr
XM_011512231.1:c.2989G>A	XP_011510533.1:p.Ala997Thr
XM_011512232.1:c.2977G>A	XP_011510534.1:p.Ala993Thr
NM_014795.4:c.2998G>A MANE Select	NP_055610.1:p.Ala1000Thr
NM_001171653.2:c.2926G>A	NP_001165124.1:p.Ala976Thr